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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 3, 2024. (Total: 232098Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Afibrinogenemia and FGA[original query]
Diagnosis of congenital fibrinogen disorders.
Annales de biologie clinique 2016 Aug 74 (4): 405-412.
Lebreton Aurélien, Casini Alessand
Mutational Epidemiology of Congenital Fibrinogen Disorders.
Thrombosis and haemostasis 2018 10 118 (11): 1867-1874.
Casini Alessandro, Blondon Marc, Tintillier Veronique, Goodyer Matthew, Sezgin Melike E, Gunes Adalet M, Hanss Michel, de Moerloose Philippe, Neerman-Arbez Margueri
Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
Thrombosis research 2019 9 182 133-140.
Wypasek Ewa, Klukowska Anna, Zdziarska Joanna, Zawilska Krystyna, Treli?ski Jacek, Iwaniec Teresa, Mital Andrzej, Pietrys Danuta, Sydor Wojciech, Neerman-Arbez Marguerite, Undas Anet
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
International journal of laboratory hematology 2020 7 42 (5): 619-627.
Tavasoli Behnaz, Safa Majid, Dorgalaleh Akbar, Ghasemi Jahan B, Rezaei Makhouri Farahnaz, Rezvani Mohammad R, Ahmadi Abbas, Tabibian Shadi, Jazebi Mohammad, Baghaipour Mohammad R, Zaker Farh
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
Haemophilia : the official journal of the World Federation of Hemophilia 2021 8 27 (6): 1022-1027.
Shen Ming-Ching, Wang Jiaan-Der, Tsai Woei, Lin Ching-Yeh, Lin Jen-Shiou, Kuo Su-Feng, Lin Po-Te, Huang Ying-Chih, Hung Mei-H
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2021 7 60 (6): 103203.
Mohsenian Samin, Seidizadeh Omid, Mirakhorli Mojgan, Jazebi Mohammad, Azarkeivan Azi
[Clinical phenotypes and genotypes of congenital fibrinogen disorder: an analysis of 16 children].
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2024 8 26 (8): 840-844.
Min Wang, Tian-Ping Chen, Ao-Shuang Jiang, Ying-Hui Zhao, Cheng-Lin Zhu, Nan Wei, Yu-Ting Jin, Li-Jun
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